A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256097



Internal ID21398529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:145693822..145694599hg38UCSC Ensembl
chr4:146614974..146615751hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38778
hg19778
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730167
Supporting Variants
SamplesHG00514
Known GenesC4orf51
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256097
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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